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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Administrative data

Description of key information

One acute oral toxicity study (K1) and one acute dermal toxicity study (K1) are available. Both studies are carried out under GLP conditions and according to  internationally accepted study protocols.
Under the conditions of the acute oral toxicity test, the acute oral LD50 of the test substance was determined to be greater than 5000 mg/kg bw in the rat.
Under the conditions of the acute dermal toxicity test, the acute dermal LD50 of the test substance was determined to be greater than 2000 mg/kg bw in the rabbit.
The test substance therefore is considered practically nontoxic.

Key value for chemical safety assessment

Additional information

Justification for classification or non-classification

No oral or dermal toxicity observed in limit tests at maximal required test doses.

Conclusive, but not sufficient for classification